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Federal Register: Effective Date of Requirement for Premarket Approval for Two Class III Preamendments Devices

Posted Jan 18 2013 12:00am
The FDA is proposing to require the filing of a premarket approval application (PMA) or a notice of completion of a product development protocol (PDP) for the following two class III preamendments devices: Hip joint metal/metal semi-constrained, with a...
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